FACILE SOL–GEL SYNTHESIS OF Li[Li0.2Mn0.56Ni0.16Co0.08]O2 AS IMPROVED CATHODE MATERIAL FOR LITHIUM-ION BATTERIES

2013 ◽  
Vol 01 (04) ◽  
pp. 1340015
Author(s):  
WENJUAN HAO ◽  
HAN CHEN ◽  
YANHONG WANG ◽  
HANHUI ZHAN ◽  
QIANGQIANG TAN ◽  
...  

Li [ Li 0.2 Mn 0.56 Ni 0.16 Co 0.08] O 2 cathode materials for Li -ion batteries were synthesized by a facile sol–gel method followed by calcination at various temperatures (700°C, 800°C and 900°C). Lithium acetate dihydrate, manganese (II) acetate tetrahydrate, nickel (II) acetate tetrahydrate and cobalt (II) acetate tetrahydrate are employed as the metal precursors, and citric acid monohydrate as the chelating agent. For the obtained Li [ Li 0.2 Mn 0.56 Ni 0.16 Co 0.08] O 2 materials, the metal components existed in the form of Mn 4+, Ni 2+ and Co 3+, and their molar ratio was in good agreement with 0.56 : 0.16 : 0.08. The calcination temperature played an important role in the particle size, crystallinity and further electrochemical properties of the cathode materials. The Li [ Li 0.2 Mn 0.56 Ni 0.16 Co 0.08] O 2 material calcined at 800°C for 6 h showed the best electrochemical performances. Its discharge specific capacities cycled at 0.1 C, 0.5 C, 1 C and 2 C rates were 266.0 mAh g−1, 243.1 mAh g−1, 218.2 mAh g−1 and 192.9 mAh g−1, respectively. When recovered to 0.1 C rate, the discharge specific capacity was 260.2 mAh g−1 and the capacity loss is only 2.2%. This work demonstrates that the sol–gel method is a facile route to prepare high performance Li [ Li 0.2 Mn 0.56 Ni 0.16 Co 0.08] O 2 cathode materials for Li -ion batteries.

2016 ◽  
Vol 42 (1) ◽  
pp. 1897-1902 ◽  
Author(s):  
Li Yang ◽  
Guoxi Xi ◽  
Tianjun Lou ◽  
Xinsheng Wang ◽  
Jingjing Wang ◽  
...  

2010 ◽  
Vol 156-157 ◽  
pp. 1219-1222 ◽  
Author(s):  
Bo Quan Jiang ◽  
Shu Fen Hu ◽  
Min Wei Wang

The lithium vanadium phosphate (Li3V2(PO4)3 solid cathode materials were synthesized by microwave-heated sol-gel method using lithium hydroxide, ammonium metavanadate, phosphate and citric acid as starting materials. The test was conducted with orthogonal experiment method. The optimal conditions for (Li3V2(PO4)3 synthesis were determined to be microwave heating time of 10 min, microwave power of 700 W, Li/V molar ratio of 3.05:2.0 and pH value(gel solution) of 7.0. The synthesized (Li3V2(PO4)3 under the optimal conditions demonstrated perfect crystal growth and good electrochemical performance with initial charge/discharge specific capacity of 172.42 mAh·g-1/154.93 mAh·g-1 and discharge decay rate of 2.25 % after 50 cycles. The lithium ion diffusion coefficient was determined to be 1.434 ×10-8 cm2·s-1 by electrochemical impedance spectroscopy and mathematical models derived from simulative equivalent circuit.


2013 ◽  
Vol 2 (1) ◽  
pp. 68-72 ◽  
Author(s):  
Wei Liu ◽  
Jun Liu ◽  
Yanling Wan ◽  
Shaomin Ji ◽  
Yichun Zhou

2009 ◽  
Vol 289-292 ◽  
pp. 565-570 ◽  
Author(s):  
W. Iwaniak ◽  
J. Fritzsche ◽  
M. Zukalová ◽  
R. Winter ◽  
Martin Wilkening ◽  
...  

Spinel-type structured Li4+xTi5O12 (0 6 x 6 3 ) is actually one of the most promising anode materials for Li ion batteries. In its nanostructured form it is already used in some commercially available Li ion batteries. As was recently shown by our group (Wilkening et al., Phys. Chem. Chem. Phys. 9 (2007) 1239), Li diffusivity in microcrystalline Li4+xTi5O12 with x = 0 is rather slow. In the present contribution the Li conductivity in nanocrystalline samples of the electronic insulator Li4Ti5O12 prepared by different routes is investigated using impedance spectroscopy. The mean crystallite size of the samples is about 20 nm. The ionic conductivity of nanocrystalline Li4Ti5O12 obtained by mechanical treatment is higher by about two orders of magnitude compared to that found for a material which was prepared following a sol-gel method. The latter resembles the behaviour of the microcrystalline sample with an average particle size in the μm range rather than that of a nanocrystalline ball milled one with a mean crystallite size of about than 20 nm. The larger conductivity of the ball milled sample is ascribed to a much higher defect density generated when the particle size is reduced mechanically.


2019 ◽  
Vol 9 (2) ◽  
pp. 3866-3873

Composites of {[(1-x-y) LiFe0.333Ni0.333 Co0.333] PO4}, xLi2FePO4F and yLiCoPO4system were synthesized using the sol-gel method. Stoichiometric weights of the mole-fraction of LiOH, FeCl2·4H2O and H3PO4, LiCl, Ni(NO3)2⋅6H2O, Co(Ac)2⋅4H2O, as starting materials of lithium, Iron, Nickel , and Cobalt, in 7 samples of the system, respectively. We exhibited Li1.167 Ni0.222 Co0.389 Fe0.388 PO4 is the best composition for cathode material in this study. Obviously, the used weight of cobalt in these samples is lower compared with LiCoO2 that is an advantage in view point of cost in this study. Charge-discharge haracteristics of the mentioned cathode materials were investigated by performing cycle tests in the range of 2.4–3.8 V (versus Li/Li+). Our results confirmed, although these kind systems can help for removing the disadvantage of cobalt which mainly is its cost and toxic, the performance of these kind systems are similar to the commercial cathode materials in Lithium Ion batteries (LIBs).


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Hailang Zhang

Prospective cathode materialsLiNi0.7–xMgxCo0.3O2(0≤x≤0.1) for a lithium-ion secondary battery were synthesized using a sol-gel method. The structural and electrochemical properties were examined by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), cyclic voltammetry(CV), and charge-discharge tests. The results show that theLiNi0.7–xMgxCo0.3O2maintains theα-NaFeO2type layered structure regardless of the magnesium content in the rangex⩽0.1. On the other hand, Mg-doping improves the capacity retention well. Besides, the Mg-doping promotes the diffusion of Li+in LiNi0.7Co0.3O2. Moreover, Mg-doping suppresses the phase transitions that usually occur in LiNiO2during cycling and improves the charge-discharge reversibility of Li/LiNi0.7Co0.3O2. High temperature cycling performance of the cathode at 55.5°C is also improved by Mg-doping, which is possibly attributed to the total stronger metal-oxygen bonding and the enhanced structure stability of those delithiated Mg-doped cathodes during cycling.


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